Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1037084691
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 0
dbSNP: rs1037084691
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv
CUI: C1691215
Disease: Penile hypospadias
Penile hypospadias 		0.010 1.000 1 2019 2019
dbSNP: rs1037084691
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv
CUI: C0452148
Disease: Hypospadias, perineal
Hypospadias, perineal 		0.010 1.000 1 2019 2019
dbSNP: rs1037084691
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv
CUI: C0848558
Disease: Hypospadias
Hypospadias 		0.010 1.000 1 2019 2019
dbSNP: rs1037084691
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.010 1.000 1 2015 2015